Heparin therapy in sepsis and sepsis-associated disseminated intravascular coagulation: a systematic review and meta-analysis
Sepsis is a life-threatening condition that affects 49 million people annually. Managing sepsis-associated coagulopathy poses a significant challenge due to its high mortality rates in intensive care. Recent reports suggest that administering heparin may offer potential survival benefits in sepsis a...
Saved in:
Published in | Thrombosis journal Vol. 22; no. 1; pp. 84 - 8 |
---|---|
Main Authors | , , , , , , |
Format | Journal Article |
Language | English |
Published |
England
BioMed Central Ltd
30.09.2024
BioMed Central BMC |
Subjects | |
Online Access | Get full text |
ISSN | 1477-9560 1477-9560 |
DOI | 10.1186/s12959-024-00653-0 |
Cover
Loading…
Abstract | Sepsis is a life-threatening condition that affects 49 million people annually. Managing sepsis-associated coagulopathy poses a significant challenge due to its high mortality rates in intensive care. Recent reports suggest that administering heparin may offer potential survival benefits in sepsis and coronavirus disease cases. However, there is currently no established evidence supporting the use of heparin for sepsis. Thus, in this study, we aimed to assess the efficacy of heparin administration in patients with sepsis.
A systematic review was conducted following the PRISMA guidelines. The searches included MEDLINE, Cochrane, and Japanese databases up to January 2023. The inclusion criteria consisted of randomized control trials (RCTs) involving adult sepsis patients receiving heparin. The risk of bias was assessed using RoB2, and the data extraction included 28-day mortality and bleeding complications.
Out of 1733 initial articles, only three studies met the inclusion criteria. The analysis, which included 426 patients, showed no significant difference in 28-day and in-hospital mortality between the heparin and control groups (risk ratio [RR] = 0.86, 95% confidence interval [CI]: 0.60-1.24). Subgroup analysis of sepsis-associated disseminated intravascular coagulation (DIC) patients (n = 109) also did not show a significant reduction in mortality (RR = 0.84, 95% CI: 0.51-1.38). Heterogeneity was zero, and no publication bias was observed. Additionally, there was significant difference in bleeding complications (RR = 0.49, 95% CI: 0.24-0.99, p = 0.047).
This meta-analysis did not demonstrate a survival benefit of heparin administration in patients with sepsis and sepsis-associated DIC. Further investigation into the potential benefits of heparin is warranted. Moreover, the analysis revealed no increase in bleeding risks with heparin administration; instead, a significant reduction in the risk of bleeding was noted.
This review was preregistered with PROSPERO (registration: CRD42023385091). |
---|---|
AbstractList | Background Sepsis is a life-threatening condition that affects 49 million people annually. Managing sepsis-associated coagulopathy poses a significant challenge due to its high mortality rates in intensive care. Recent reports suggest that administering heparin may offer potential survival benefits in sepsis and coronavirus disease cases. However, there is currently no established evidence supporting the use of heparin for sepsis. Thus, in this study, we aimed to assess the efficacy of heparin administration in patients with sepsis. Methods A systematic review was conducted following the PRISMA guidelines. The searches included MEDLINE, Cochrane, and Japanese databases up to January 2023. The inclusion criteria consisted of randomized control trials (RCTs) involving adult sepsis patients receiving heparin. The risk of bias was assessed using RoB2, and the data extraction included 28-day mortality and bleeding complications. Results Out of 1733 initial articles, only three studies met the inclusion criteria. The analysis, which included 426 patients, showed no significant difference in 28-day and in-hospital mortality between the heparin and control groups (risk ratio [RR] = 0.86, 95% confidence interval [CI]: 0.60-1.24). Subgroup analysis of sepsis-associated disseminated intravascular coagulation (DIC) patients (n = 109) also did not show a significant reduction in mortality (RR = 0.84, 95% CI: 0.51-1.38). Heterogeneity was zero, and no publication bias was observed. Additionally, there was significant difference in bleeding complications (RR = 0.49, 95% CI: 0.24-0.99, p = 0.047). Conclusions This meta-analysis did not demonstrate a survival benefit of heparin administration in patients with sepsis and sepsis-associated DIC. Further investigation into the potential benefits of heparin is warranted. Moreover, the analysis revealed no increase in bleeding risks with heparin administration; instead, a significant reduction in the risk of bleeding was noted. Trial registration This review was preregistered with PROSPERO (registration: CRD42023385091). Keywords: Sepsis, Disseminated intravascular coagulation, Heparin, Low molecular weight heparin Sepsis is a life-threatening condition that affects 49 million people annually. Managing sepsis-associated coagulopathy poses a significant challenge due to its high mortality rates in intensive care. Recent reports suggest that administering heparin may offer potential survival benefits in sepsis and coronavirus disease cases. However, there is currently no established evidence supporting the use of heparin for sepsis. Thus, in this study, we aimed to assess the efficacy of heparin administration in patients with sepsis. A systematic review was conducted following the PRISMA guidelines. The searches included MEDLINE, Cochrane, and Japanese databases up to January 2023. The inclusion criteria consisted of randomized control trials (RCTs) involving adult sepsis patients receiving heparin. The risk of bias was assessed using RoB2, and the data extraction included 28-day mortality and bleeding complications. Out of 1733 initial articles, only three studies met the inclusion criteria. The analysis, which included 426 patients, showed no significant difference in 28-day and in-hospital mortality between the heparin and control groups (risk ratio [RR] = 0.86, 95% confidence interval [CI]: 0.60-1.24). Subgroup analysis of sepsis-associated disseminated intravascular coagulation (DIC) patients (n = 109) also did not show a significant reduction in mortality (RR = 0.84, 95% CI: 0.51-1.38). Heterogeneity was zero, and no publication bias was observed. Additionally, there was significant difference in bleeding complications (RR = 0.49, 95% CI: 0.24-0.99, p = 0.047). This meta-analysis did not demonstrate a survival benefit of heparin administration in patients with sepsis and sepsis-associated DIC. Further investigation into the potential benefits of heparin is warranted. Moreover, the analysis revealed no increase in bleeding risks with heparin administration; instead, a significant reduction in the risk of bleeding was noted. Sepsis is a life-threatening condition that affects 49 million people annually. Managing sepsis-associated coagulopathy poses a significant challenge due to its high mortality rates in intensive care. Recent reports suggest that administering heparin may offer potential survival benefits in sepsis and coronavirus disease cases. However, there is currently no established evidence supporting the use of heparin for sepsis. Thus, in this study, we aimed to assess the efficacy of heparin administration in patients with sepsis. A systematic review was conducted following the PRISMA guidelines. The searches included MEDLINE, Cochrane, and Japanese databases up to January 2023. The inclusion criteria consisted of randomized control trials (RCTs) involving adult sepsis patients receiving heparin. The risk of bias was assessed using RoB2, and the data extraction included 28-day mortality and bleeding complications. Out of 1733 initial articles, only three studies met the inclusion criteria. The analysis, which included 426 patients, showed no significant difference in 28-day and in-hospital mortality between the heparin and control groups (risk ratio [RR] = 0.86, 95% confidence interval [CI]: 0.60-1.24). Subgroup analysis of sepsis-associated disseminated intravascular coagulation (DIC) patients (n = 109) also did not show a significant reduction in mortality (RR = 0.84, 95% CI: 0.51-1.38). Heterogeneity was zero, and no publication bias was observed. Additionally, there was significant difference in bleeding complications (RR = 0.49, 95% CI: 0.24-0.99, p = 0.047). This meta-analysis did not demonstrate a survival benefit of heparin administration in patients with sepsis and sepsis-associated DIC. Further investigation into the potential benefits of heparin is warranted. Moreover, the analysis revealed no increase in bleeding risks with heparin administration; instead, a significant reduction in the risk of bleeding was noted. This review was preregistered with PROSPERO (registration: CRD42023385091). Abstract Background Sepsis is a life-threatening condition that affects 49 million people annually. Managing sepsis-associated coagulopathy poses a significant challenge due to its high mortality rates in intensive care. Recent reports suggest that administering heparin may offer potential survival benefits in sepsis and coronavirus disease cases. However, there is currently no established evidence supporting the use of heparin for sepsis. Thus, in this study, we aimed to assess the efficacy of heparin administration in patients with sepsis. Methods A systematic review was conducted following the PRISMA guidelines. The searches included MEDLINE, Cochrane, and Japanese databases up to January 2023. The inclusion criteria consisted of randomized control trials (RCTs) involving adult sepsis patients receiving heparin. The risk of bias was assessed using RoB2, and the data extraction included 28-day mortality and bleeding complications. Results Out of 1733 initial articles, only three studies met the inclusion criteria. The analysis, which included 426 patients, showed no significant difference in 28-day and in-hospital mortality between the heparin and control groups (risk ratio [RR] = 0.86, 95% confidence interval [CI]: 0.60–1.24). Subgroup analysis of sepsis-associated disseminated intravascular coagulation (DIC) patients (n = 109) also did not show a significant reduction in mortality (RR = 0.84, 95% CI: 0.51–1.38). Heterogeneity was zero, and no publication bias was observed. Additionally, there was significant difference in bleeding complications (RR = 0.49, 95% CI: 0.24–0.99, p = 0.047). Conclusions This meta-analysis did not demonstrate a survival benefit of heparin administration in patients with sepsis and sepsis-associated DIC. Further investigation into the potential benefits of heparin is warranted. Moreover, the analysis revealed no increase in bleeding risks with heparin administration; instead, a significant reduction in the risk of bleeding was noted. Trial registration This review was preregistered with PROSPERO (registration: CRD42023385091). Sepsis is a life-threatening condition that affects 49 million people annually. Managing sepsis-associated coagulopathy poses a significant challenge due to its high mortality rates in intensive care. Recent reports suggest that administering heparin may offer potential survival benefits in sepsis and coronavirus disease cases. However, there is currently no established evidence supporting the use of heparin for sepsis. Thus, in this study, we aimed to assess the efficacy of heparin administration in patients with sepsis.BACKGROUNDSepsis is a life-threatening condition that affects 49 million people annually. Managing sepsis-associated coagulopathy poses a significant challenge due to its high mortality rates in intensive care. Recent reports suggest that administering heparin may offer potential survival benefits in sepsis and coronavirus disease cases. However, there is currently no established evidence supporting the use of heparin for sepsis. Thus, in this study, we aimed to assess the efficacy of heparin administration in patients with sepsis.A systematic review was conducted following the PRISMA guidelines. The searches included MEDLINE, Cochrane, and Japanese databases up to January 2023. The inclusion criteria consisted of randomized control trials (RCTs) involving adult sepsis patients receiving heparin. The risk of bias was assessed using RoB2, and the data extraction included 28-day mortality and bleeding complications.METHODSA systematic review was conducted following the PRISMA guidelines. The searches included MEDLINE, Cochrane, and Japanese databases up to January 2023. The inclusion criteria consisted of randomized control trials (RCTs) involving adult sepsis patients receiving heparin. The risk of bias was assessed using RoB2, and the data extraction included 28-day mortality and bleeding complications.Out of 1733 initial articles, only three studies met the inclusion criteria. The analysis, which included 426 patients, showed no significant difference in 28-day and in-hospital mortality between the heparin and control groups (risk ratio [RR] = 0.86, 95% confidence interval [CI]: 0.60-1.24). Subgroup analysis of sepsis-associated disseminated intravascular coagulation (DIC) patients (n = 109) also did not show a significant reduction in mortality (RR = 0.84, 95% CI: 0.51-1.38). Heterogeneity was zero, and no publication bias was observed. Additionally, there was significant difference in bleeding complications (RR = 0.49, 95% CI: 0.24-0.99, p = 0.047).RESULTSOut of 1733 initial articles, only three studies met the inclusion criteria. The analysis, which included 426 patients, showed no significant difference in 28-day and in-hospital mortality between the heparin and control groups (risk ratio [RR] = 0.86, 95% confidence interval [CI]: 0.60-1.24). Subgroup analysis of sepsis-associated disseminated intravascular coagulation (DIC) patients (n = 109) also did not show a significant reduction in mortality (RR = 0.84, 95% CI: 0.51-1.38). Heterogeneity was zero, and no publication bias was observed. Additionally, there was significant difference in bleeding complications (RR = 0.49, 95% CI: 0.24-0.99, p = 0.047).This meta-analysis did not demonstrate a survival benefit of heparin administration in patients with sepsis and sepsis-associated DIC. Further investigation into the potential benefits of heparin is warranted. Moreover, the analysis revealed no increase in bleeding risks with heparin administration; instead, a significant reduction in the risk of bleeding was noted.CONCLUSIONSThis meta-analysis did not demonstrate a survival benefit of heparin administration in patients with sepsis and sepsis-associated DIC. Further investigation into the potential benefits of heparin is warranted. Moreover, the analysis revealed no increase in bleeding risks with heparin administration; instead, a significant reduction in the risk of bleeding was noted.This review was preregistered with PROSPERO (registration: CRD42023385091).TRIAL REGISTRATIONThis review was preregistered with PROSPERO (registration: CRD42023385091). |
ArticleNumber | 84 |
Audience | Academic |
Author | Koami, Hiroyuki Iba, Toshiaki Totoki, Takaaki Ito, Takashi Yamakawa, Kazuma Wada, Takeshi Makino, Yuto |
Author_xml | – sequence: 1 givenname: Takaaki surname: Totoki fullname: Totoki, Takaaki – sequence: 2 givenname: Hiroyuki surname: Koami fullname: Koami, Hiroyuki – sequence: 3 givenname: Yuto surname: Makino fullname: Makino, Yuto – sequence: 4 givenname: Takeshi surname: Wada fullname: Wada, Takeshi – sequence: 5 givenname: Takashi surname: Ito fullname: Ito, Takashi – sequence: 6 givenname: Kazuma surname: Yamakawa fullname: Yamakawa, Kazuma – sequence: 7 givenname: Toshiaki surname: Iba fullname: Iba, Toshiaki |
BackLink | https://www.ncbi.nlm.nih.gov/pubmed/39350146$$D View this record in MEDLINE/PubMed |
BookMark | eNp9kktv1DAUhSNURB_wB1igSGzYpFzHjyRsUFUBrVSJDawtP66nrhJ7sDODZsF_x_Og6iCEsvC1c-6ne-xzXp2EGLCqXhO4JKQX7zNpBz400LIGQHDawLPqjLCuawYu4ORJfVqd5_wA0LZDy19Up3SgHAgTZ9WvG1yq5EM932NSy01dyozL7HOtgj2Ujco5Gq9mtLX1OePkw27jw5zUWmWzGlWqTVSLUsw-hg-1qvMmzziVrakTrj3-3BEnnFWjgho3Bfyyeu7UmPHVYb2ovn_-9O36prn7-uX2-uquMZyKuRkoUdQNgqNG0lNDqXXggHc4WEcJEVoYBpxx1vXAWtCEgtF9Z3ULTAPQi-p2z7VRPchl8pNKGxmVl7uDmBZSpTLoiFIQ2lmFFgbGmCVWOz60A20d1xqcNoX1cc9arvSE1uD2DsYj6PGf4O_lIq4lIYxB34tCeHcgpPhjhXmWk88Gx1EFjKssiyMiaLHSFenbvXShymw-uFiQZiuXVz2BrrgmW3uX_1CVz5aXMiU0zpfzo4Y3Tz08Dv8nF0XQ7gUmxZwTukcJAbkNn9yHT5bwyV345Jba_9Vk_LyLQxnHj_9r_Q391t9M |
CitedBy_id | crossref_primary_10_3389_fphar_2025_1518716 |
Cites_doi | 10.1001/jama.2016.0287 10.1055/s-0040-1715460 10.1177/10760296211053313 10.1016/j.amjcard.2009.10.043 10.1055/s-0040-1720978 10.1097/CCM.0b013e31819c06bc 10.1097/CCM.0b013e3181953c5e 10.1016/j.imbio.2014.06.005 10.1038/s41577-021-00536-9 10.1038/srep25984 10.2169/internalmedicine.1923-18 10.3389/fmed.2023.1157775 10.1097/CCM.0000000000000763 10.21037/apm-21-169 10.1186/s12871-021-01545-w 10.1016/S0140-6736(19)32989-7 10.1097/CCM.0000000000005337 10.3892/etm.2013.1466 10.1002/path.1597 10.1111/jth.13230 10.1097/00003246-199206000-00025 10.1001/jamainternmed.2021.6203 10.1186/s13054-014-0563-4 10.1016/j.thromres.2016.07.016 10.1007/s00068-022-02044-4 10.1136/bmj.n71 10.1097/ALN.0000000000003122 10.3389/fphar.2023.1173893 10.1111/jth.14975 10.1001/jama.2020.18618 10.1136/bmj.l4898 10.1007/s00134-003-1662-x |
ContentType | Journal Article |
Copyright | 2024. The Author(s). COPYRIGHT 2024 BioMed Central Ltd. The Author(s) 2024 2024 |
Copyright_xml | – notice: 2024. The Author(s). – notice: COPYRIGHT 2024 BioMed Central Ltd. – notice: The Author(s) 2024 2024 |
DBID | AAYXX CITATION NPM 7X8 5PM DOA |
DOI | 10.1186/s12959-024-00653-0 |
DatabaseName | CrossRef PubMed MEDLINE - Academic PubMed Central (Full Participant titles) DOAJ Directory of Open Access Journals |
DatabaseTitle | CrossRef PubMed MEDLINE - Academic |
DatabaseTitleList | PubMed MEDLINE - Academic |
Database_xml | – sequence: 1 dbid: DOA name: DOAJ Directory of Open Access Journals url: https://www.doaj.org/ sourceTypes: Open Website – sequence: 2 dbid: NPM name: PubMed url: https://proxy.k.utb.cz/login?url=http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?db=PubMed sourceTypes: Index Database |
DeliveryMethod | fulltext_linktorsrc |
Discipline | Medicine |
EISSN | 1477-9560 |
EndPage | 8 |
ExternalDocumentID | oai_doaj_org_article_6137daed09444d1dbf592932f5bb0fbc PMC11440886 A810740510 39350146 10_1186_s12959_024_00653_0 |
Genre | Journal Article |
GeographicLocations | Japan |
GeographicLocations_xml | – name: Japan |
GroupedDBID | --- 0R~ 29Q 2WC 53G 5VS 6PF 7X7 8FI 8FJ AAFWJ AAJSJ AASML AAWTL AAYXX ABDBF ABUWG ACGFS ACIHN ACUHS ADBBV ADRAZ ADUKV AEAQA AFKRA AFPKN AHBYD AHMBA AHYZX ALIPV ALMA_UNASSIGNED_HOLDINGS AMKLP AMTXH AOIJS BAPOH BAWUL BCNDV BENPR BFQNJ BMC BPHCQ BVXVI C6C CCPQU CITATION CS3 DIK E3Z EBD EBLON EBS ESX F5P FYUFA GROUPED_DOAJ GX1 HMCUK HYE IAO IHR INH INR ITC KQ8 M48 M~E O5R O5S OK1 OVT PGMZT PHGZM PHGZT PIMPY PQQKQ PROAC RBZ RNS ROL RPM RSV SMD SOJ TR2 TUS UKHRP W2D WOQ WOW XSB ~8M NPM PMFND 7X8 5PM PUEGO |
ID | FETCH-LOGICAL-c536t-931a3f965ebe183c33df0f057e9df3116b6c405454780420b130cb87db204b003 |
IEDL.DBID | M48 |
ISSN | 1477-9560 |
IngestDate | Wed Aug 27 01:31:56 EDT 2025 Thu Aug 21 18:31:09 EDT 2025 Thu Jul 10 17:49:40 EDT 2025 Tue Jun 17 22:06:17 EDT 2025 Tue Jun 10 21:00:48 EDT 2025 Thu Apr 03 06:55:27 EDT 2025 Tue Jul 01 04:21:13 EDT 2025 Thu Apr 24 23:09:06 EDT 2025 |
IsDoiOpenAccess | true |
IsOpenAccess | true |
IsPeerReviewed | true |
IsScholarly | true |
Issue | 1 |
Keywords | Disseminated intravascular coagulation Low molecular weight heparin Sepsis Heparin |
Language | English |
License | 2024. The Author(s). Open Access This article is licensed under a Creative Commons Attribution-NonCommercial-NoDerivatives 4.0 International License, which permits any non-commercial use, sharing, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if you modified the licensed material. You do not have permission under this licence to share adapted material derived from this article or parts of it. The images or other third party material in this article are included in the article’s Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by-nc-nd/4.0/. |
LinkModel | DirectLink |
MergedId | FETCHMERGED-LOGICAL-c536t-931a3f965ebe183c33df0f057e9df3116b6c405454780420b130cb87db204b003 |
Notes | ObjectType-Article-1 SourceType-Scholarly Journals-1 ObjectType-Feature-2 content type line 23 |
OpenAccessLink | http://journals.scholarsportal.info/openUrl.xqy?doi=10.1186/s12959-024-00653-0 |
PMID | 39350146 |
PQID | 3111637807 |
PQPubID | 23479 |
PageCount | 8 |
ParticipantIDs | doaj_primary_oai_doaj_org_article_6137daed09444d1dbf592932f5bb0fbc pubmedcentral_primary_oai_pubmedcentral_nih_gov_11440886 proquest_miscellaneous_3111637807 gale_infotracmisc_A810740510 gale_infotracacademiconefile_A810740510 pubmed_primary_39350146 crossref_primary_10_1186_s12959_024_00653_0 crossref_citationtrail_10_1186_s12959_024_00653_0 |
ProviderPackageCode | CITATION AAYXX |
PublicationCentury | 2000 |
PublicationDate | 2024-09-30 |
PublicationDateYYYYMMDD | 2024-09-30 |
PublicationDate_xml | – month: 09 year: 2024 text: 2024-09-30 day: 30 |
PublicationDecade | 2020 |
PublicationPlace | England |
PublicationPlace_xml | – name: England – name: London |
PublicationTitle | Thrombosis journal |
PublicationTitleAlternate | Thromb J |
PublicationYear | 2024 |
Publisher | BioMed Central Ltd BioMed Central BMC |
Publisher_xml | – name: BioMed Central Ltd – name: BioMed Central – name: BMC |
References | M Singer (653_CR32) 2016; 315 Z Zhang (653_CR4) 2023; 10 J Weng (653_CR19) 2021; 27 S Fu (653_CR14) 2022; 22 N Morita (653_CR27) 2019; 58 KF To (653_CR23) 2004; 203 C Wang (653_CR10) 2014; 18 Y Umemura (653_CR25) 2016; 14 P Liasidis (653_CR28) 2023; 49 X Li (653_CR13) 2021; 10 653_CR30 F Jaimes (653_CR17) 2009; 37 X Li (653_CR6) 2014; 219 HM Oudemans-van Straaten (653_CR18) 2009; 37 A Zarbock (653_CR20) 2020; 324 MM Levy (653_CR31) 2003; 29 Y Fan (653_CR12) 2016; 6 MJ Page (653_CR15) 2021; 372 JAC Sterne (653_CR16) 2019; 366 AC Spyropoulos (653_CR2) 2021; 181 DMH Beurskens (653_CR5) 2020; 120 L Evans (653_CR7) 2021; 49 T Iba (653_CR24) 2020; 18 XL Liu (653_CR8) 2014; 7 KE Rudd (653_CR1) 2020; 395 HH Billett (653_CR3) 2020; 120 YJ Shimada (653_CR29) 2010; 105 JJ Huang (653_CR9) 2023; 14 R Zarychanski (653_CR11) 2015; 43 T Iba (653_CR22) 2020; 132 A Bonaventura (653_CR21) 2021; 21 T Iba (653_CR26) 2016; 145 |
References_xml | – volume: 315 start-page: 801 issue: 8 year: 2016 ident: 653_CR32 publication-title: JAMA doi: 10.1001/jama.2016.0287 – volume: 120 start-page: 1371 issue: 10 year: 2020 ident: 653_CR5 publication-title: Thromb Haemost doi: 10.1055/s-0040-1715460 – volume: 27 start-page: 107602962110533 year: 2021 ident: 653_CR19 publication-title: Clin Appl Thromb Hemost doi: 10.1177/10760296211053313 – volume: 105 start-page: 629 issue: 5 year: 2010 ident: 653_CR29 publication-title: Am J Cardiol doi: 10.1016/j.amjcard.2009.10.043 – volume: 120 start-page: 1691 issue: 12 year: 2020 ident: 653_CR3 publication-title: Thromb Haemost doi: 10.1055/s-0040-1720978 – volume: 37 start-page: 1185 issue: 4 year: 2009 ident: 653_CR17 publication-title: Crit Care Med doi: 10.1097/CCM.0b013e31819c06bc – volume: 37 start-page: 545 issue: 2 year: 2009 ident: 653_CR18 publication-title: Crit Care Med doi: 10.1097/CCM.0b013e3181953c5e – volume: 219 start-page: 778 issue: 10 year: 2014 ident: 653_CR6 publication-title: Immunobiology doi: 10.1016/j.imbio.2014.06.005 – volume: 21 start-page: 319 issue: 5 year: 2021 ident: 653_CR21 publication-title: Nat Rev Immunol doi: 10.1038/s41577-021-00536-9 – volume: 6 start-page: 25984 year: 2016 ident: 653_CR12 publication-title: Sci Rep doi: 10.1038/srep25984 – volume: 58 start-page: 907 issue: 7 year: 2019 ident: 653_CR27 publication-title: Intern Med doi: 10.2169/internalmedicine.1923-18 – volume: 10 start-page: 1157775 year: 2023 ident: 653_CR4 publication-title: Front Med (Lausanne) doi: 10.3389/fmed.2023.1157775 – volume: 43 start-page: 511 issue: 3 year: 2015 ident: 653_CR11 publication-title: Crit Care Med doi: 10.1097/CCM.0000000000000763 – volume: 10 start-page: 3115 issue: 3 year: 2021 ident: 653_CR13 publication-title: Ann Palliat Med doi: 10.21037/apm-21-169 – volume: 22 start-page: 28 issue: 1 year: 2022 ident: 653_CR14 publication-title: BMC Anesthesiol doi: 10.1186/s12871-021-01545-w – volume: 395 start-page: 200 issue: 10219 year: 2020 ident: 653_CR1 publication-title: Lancet doi: 10.1016/S0140-6736(19)32989-7 – volume: 49 start-page: e1063 issue: 11 year: 2021 ident: 653_CR7 publication-title: Crit Care Med doi: 10.1097/CCM.0000000000005337 – volume: 7 start-page: 604 issue: 3 year: 2014 ident: 653_CR8 publication-title: Exp Ther Med doi: 10.3892/etm.2013.1466 – volume: 203 start-page: 740 issue: 3 year: 2004 ident: 653_CR23 publication-title: J Pathol doi: 10.1002/path.1597 – volume: 14 start-page: 518 issue: 3 year: 2016 ident: 653_CR25 publication-title: J Thromb Haemost doi: 10.1111/jth.13230 – ident: 653_CR30 doi: 10.1097/00003246-199206000-00025 – volume: 181 start-page: 1612 issue: 12 year: 2021 ident: 653_CR2 publication-title: JAMA Intern Med doi: 10.1001/jamainternmed.2021.6203 – volume: 18 start-page: 563 issue: 5 year: 2014 ident: 653_CR10 publication-title: Crit Care doi: 10.1186/s13054-014-0563-4 – volume: 145 start-page: 46 year: 2016 ident: 653_CR26 publication-title: Thromb Res doi: 10.1016/j.thromres.2016.07.016 – volume: 49 start-page: 241 issue: 1 year: 2023 ident: 653_CR28 publication-title: Eur J Trauma Emerg Surg doi: 10.1007/s00068-022-02044-4 – volume: 372 year: 2021 ident: 653_CR15 publication-title: BMJ doi: 10.1136/bmj.n71 – volume: 132 start-page: 1238 issue: 5 year: 2020 ident: 653_CR22 publication-title: Anesthesiology doi: 10.1097/ALN.0000000000003122 – volume: 14 start-page: 1173893 year: 2023 ident: 653_CR9 publication-title: Front Pharmacol doi: 10.3389/fphar.2023.1173893 – volume: 18 start-page: 2103 issue: 9 year: 2020 ident: 653_CR24 publication-title: J Thromb Haemost doi: 10.1111/jth.14975 – volume: 324 start-page: 1629 issue: 16 year: 2020 ident: 653_CR20 publication-title: JAMA doi: 10.1001/jama.2020.18618 – volume: 366 start-page: l4898 year: 2019 ident: 653_CR16 publication-title: BMJ doi: 10.1136/bmj.l4898 – volume: 29 start-page: 530 issue: 4 year: 2003 ident: 653_CR31 publication-title: Intensive Care Med doi: 10.1007/s00134-003-1662-x |
SSID | ssj0022925 |
Score | 2.3427682 |
Snippet | Sepsis is a life-threatening condition that affects 49 million people annually. Managing sepsis-associated coagulopathy poses a significant challenge due to... Background Sepsis is a life-threatening condition that affects 49 million people annually. Managing sepsis-associated coagulopathy poses a significant... Abstract Background Sepsis is a life-threatening condition that affects 49 million people annually. Managing sepsis-associated coagulopathy poses a significant... |
SourceID | doaj pubmedcentral proquest gale pubmed crossref |
SourceType | Open Website Open Access Repository Aggregation Database Index Database Enrichment Source |
StartPage | 84 |
SubjectTerms | Analysis Coronavirus infections Coronaviruses Disseminated intravascular coagulation Health aspects Heparin Infection Japan Low molecular weight heparin Mortality Sepsis |
SummonAdditionalLinks | – databaseName: DOAJ Directory of Open Access Journals dbid: DOA link: http://utb.summon.serialssolutions.com/2.0.0/link/0/eLvHCXMwrV3Ni9UwEA-yB_EifltdlwiCBwnbNGmaelsXl4ewnlzYW8inPtC-xb497GH_d2fS9PmKoBdvbZO2yXxkJmTmN4S8ceAlRy4Si72XTLrGMm19YL7pLI_gJ_EGs5HPP6vVhfx02V7ulfrCmLAJHngi3DGYmy7YGGAbImXgwaUWLLpoUutcnZzH1Rds3ryZKlutpm_aOUVGq-MRrFrbM7BHLIOxsnphhjJa_59r8p5RWgZM7lmgswfkfnEd6ck05IfkThwekbvn5XD8MbldRSwpONApp-qGwuUYr8b1SO0QyiWzhR8x0HwWj6EweLPGf85xqdRv7NdS2Os9tfQ33jOdcl3yF3_ErWW2oJo8IRdnH7-crliprsB8K9SW9YJbkXrVAhtBr70QIdUJ3LfYhyQ4V0558OYy4Bdodu3A2nmnu-CaWuJi8JQcDJshPic0KtlZ3wfpPHBJKCd7DRzzCT7AgXMV4TOxjS_Q41gB47vJWxCtzMQgAwwymUGmrsi73TtXE_DGX3t_QB7ueiJodn4AomSKKJl_iVJF3qIEGFRtGJ63JUMBJokgWeZEY_QqrmIVOVz0BJX0i-bXswwZbMI4tiFurkcDdAUHGAjaVeTZJFO7MWOSNEL5VEQvpG0xqWXLsP6WEcE5HtFrrV78DzK8JPearCkYFHNIDrY_r-Mr8Ly27igr2S94viz9 priority: 102 providerName: Directory of Open Access Journals |
Title | Heparin therapy in sepsis and sepsis-associated disseminated intravascular coagulation: a systematic review and meta-analysis |
URI | https://www.ncbi.nlm.nih.gov/pubmed/39350146 https://www.proquest.com/docview/3111637807 https://pubmed.ncbi.nlm.nih.gov/PMC11440886 https://doaj.org/article/6137daed09444d1dbf592932f5bb0fbc |
Volume | 22 |
hasFullText | 1 |
inHoldings | 1 |
isFullTextHit | |
isPrint | |
link | http://utb.summon.serialssolutions.com/2.0.0/link/0/eLvHCXMwjV3da9swEBddC2MvY9_z1gUPBnsY2ixblq3BGM1oCYOUURYIexH6chvonC5OYX3Y_747WclqVsZegmMpsqy7051yd78j5JUBK9mzoqFeWk65yTWttXXU5pVmHuwklmM28vRYTGb887yc75BNuaO4gN2NRzusJzVbnb_9-ePqIwj8hyDwtXjXgc4qJQVtQwPUKoUj_B5opgpLOUz51quQ5zIUYWU8uC1FtkmiuXGMgaIKeP5_79rX1NYwpPKajjq6R-5G4zI96LnhPtnx7QNyexrd5w_Jr4nHooNt2mddXaVw2fmLbtGlunXxkupIMe_S4K3HYBn8ssBnbiJXU7vUp7H01_tUp38QodM-GyaM-N2vNdUR9-QRmR0dfv00obH-ArVlIdZUFkwXjRQlEBok3xaFa7IGDDwvXVMwJoywYO8FSDCQ_cyAPrSmrpzJM47bxWOy2y5b_5SkXvBKW-m4sZLzQhgua-8y28AAzGUyIWyz2MpGcHKskXGuwiGlFqonkAICqUAglSXkzfY3Fz00xz97j5GG254Iqx1uLFenKkqpAtumchomBpPkjjnTlGA-FnlTGpM1xibkNXKAQnaE6VkdcxjgJRFGSx3UGN-K-1xC9gc9QWjtoPnlhocUNmGkW-uXl52CdQUTGRa0SsiTnqe2c8Y0agT7SUg94LbBSw1b2sVZwAxn6MSva_HsPx78nNzJgyBgVMw-2V2vLv0LML3WZkRuVfNqRPbGh8dfTkbhD4xRkDH4PBl_-w1Rhy9H |
linkProvider | Scholars Portal |
openUrl | ctx_ver=Z39.88-2004&ctx_enc=info%3Aofi%2Fenc%3AUTF-8&rfr_id=info%3Asid%2Fsummon.serialssolutions.com&rft_val_fmt=info%3Aofi%2Ffmt%3Akev%3Amtx%3Ajournal&rft.genre=article&rft.atitle=Heparin+therapy+in+sepsis+and+sepsis-associated+disseminated+intravascular+coagulation%3A+a+systematic+review+and+meta-analysis&rft.jtitle=Thrombosis+journal&rft.au=Totoki%2C+Takaaki&rft.au=Koami%2C+Hiroyuki&rft.au=Makino%2C+Yuto&rft.au=Wada%2C+Takeshi&rft.date=2024-09-30&rft.issn=1477-9560&rft.eissn=1477-9560&rft.volume=22&rft.issue=1&rft.spage=84&rft_id=info:doi/10.1186%2Fs12959-024-00653-0&rft.externalDBID=NO_FULL_TEXT |
thumbnail_l | http://covers-cdn.summon.serialssolutions.com/index.aspx?isbn=/lc.gif&issn=1477-9560&client=summon |
thumbnail_m | http://covers-cdn.summon.serialssolutions.com/index.aspx?isbn=/mc.gif&issn=1477-9560&client=summon |
thumbnail_s | http://covers-cdn.summon.serialssolutions.com/index.aspx?isbn=/sc.gif&issn=1477-9560&client=summon |